1-4 of 4
Willem Ouwehand, MD PhD
Close
Sort by
Journal Articles

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

Suthesh Sivapalaratnam, MD PhD, Willem Ouwehand, MD PhD, Bridge Consortium, ThromboGenomics Consortium
Journal: Blood
Blood (2016) 128 (22): 1359.
https://doi.org/10.1182/blood.V128.22.1359.1359
Published: 2016
Journal Articles

A Dominant Gain-of-Function Mutation in Universal Tyrosine Kinase SRC Causes Enhanced Podosome Formation in a Syndrome with Thrombocytopenia, Myelofibrosis, Bleeding and Bone Pathologies

Kathleen Freson, Ernest Turro, Willem Ouwehand, MD, PhD
Journal: Blood
Blood (2015) 126 (23): LBA-7.
https://doi.org/10.1182/blood.V126.23.LBA-7.LBA-7
Published: 2015
Journal Articles

A Novel β3 Intracytoplasmic Domain Mutation Associated with Macrothrombocytopenia: Structural Analysis in Comparison with Previously Reported Cases

Paquita Nurden, MD PhD, Ernest Turro, PhD, Xavier Pillois, PhD, Daniel Greene, PhD, Willem Ouwehand, MD PhD, Alan Nurden, PhD
Journal: Blood
Blood (2014) 124 (21): 1454.
https://doi.org/10.1182/blood.V124.21.1454.1454
Published: 2014
Journal Articles

Functional Genomics in Zebrafish Permits Rapid Characterization of Novel Platelet Membrane Proteins

Isabelle I Salles, Marie N O’Connor, Nicholas A. Watkins, Adam Walker, Stephen F Garner, Chris I Jones, Iain Macauley, Michael Steward, Jaap Jan Zwaginga, Sarah L Bray, Ana Cvejic, Frank Dudbridge, Bernard de Bono, Hans Deckmyn, Derek L. Stemple, Willem Ouwehand, MD, PhD
Journal: Blood
Blood (2008) 112 (11): 2860.
https://doi.org/10.1182/blood.V112.11.2860.2860
Published: 2008